RS387906686 SCN2A

Health Risk Chr 2:165310413
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What This Variant Does
"rs387906686, also known as c.788C&gt
Associated Conditions
Episodic ataxia
type 9
Seizures
benign familial infantile
3
Epileptic encephalopathy
Developmental and epileptic encephalopathy
11
Complex neurodevelopmental disorder
Infantile spasms
SCN2A-related disorder
Inborn genetic diseases
Developmental and epileptic encephalopathy
11
Seizures
Other Variants in SCN2A
rs121917749 rs121917750 rs121917751 rs121917752 rs121917753 rs387906683 rs387906684 rs387906685 rs387906687 rs139815570
Ask Dr. Hemsworth about this variant